Canonical Allele Identifier: CA341558955

Gene: AMPD2

Linked Data

• gnomAD v4: 1-109628655-G-T
• MyVariant Identifiers: chr1:g.110171277G>T (hg19) ; chr1:g.109628655G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109628655G>T , CM000663.2:g.109628655G>T	GRCh38
NC_000001.10:g.110171277G>T , CM000663.1:g.110171277G>T	GRCh37
NC_000001.9:g.109972800G>T	NCBI36
NG_034075.1:g.13843G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256578.8:c.1420G>T	ENSP00000256578.4:p.Asp474Tyr
ENST00000358729.9:c.1420G>T	ENSP00000351573.5:p.Asp474Tyr
ENST00000369840.7:c.1420G>T	ENSP00000358855.3:p.Asp474Tyr
ENST00000474459.6:n.2039G>T
ENST00000476688.3:c.1102G>T	ENSP00000437025.2:p.Asp368Tyr
ENST00000486282.7:n.2376G>T
ENST00000524975.2:n.1901G>T
ENST00000525415.2:n.1936G>T
ENST00000526301.6:n.1483G>T
ENST00000527846.7:n.1275G>T
ENST00000528667.7:c.1420G>T MANE Select	ENSP00000436541.2:p.Asp474Tyr
ENST00000531203.6:c.1228G>T	ENSP00000431975.2:p.Asp410Tyr
ENST00000531734.6:c.1339G>T	ENSP00000433739.2:p.Asp447Tyr
ENST00000652975.2:c.*1172G>T	ENSP00000499620.2:n.*1172G>T
ENST00000654851.1:n.1262G>T
ENST00000655992.1:c.1228G>T	ENSP00000499740.1:p.Asp410Tyr
ENST00000659122.2:c.1407+160G>T	ENSP00000499621.2:n.1407+160G>T
ENST00000663749.1:c.*1167G>T	ENSP00000499739.1:n.*1167G>T
ENST00000667949.2:c.820G>T	ENSP00000499465.2:p.Asp274Tyr
ENST00000668421.1:c.*1361G>T	ENSP00000499362.1:n.*1361G>T
ENST00000679379.1:c.*1172G>T	ENSP00000505528.1:n.*1172G>T
ENST00000679593.1:c.1420G>T	ENSP00000505999.1:p.Asp474Tyr
ENST00000679880.1:n.1956G>T
ENST00000679892.1:c.*1188G>T	ENSP00000504882.1:n.*1188G>T
ENST00000679981.1:c.*1434G>T	ENSP00000506422.1:n.*1434G>T
ENST00000680132.1:c.*1370G>T	ENSP00000505950.1:n.*1370G>T
ENST00000680148.1:c.*1172G>T	ENSP00000505994.1:n.*1172G>T
ENST00000680170.1:n.2285G>T
ENST00000680192.1:n.2378G>T
ENST00000680519.1:n.1656G>T
ENST00000680531.1:c.*1167G>T	ENSP00000506332.1:n.*1167G>T
ENST00000680820.1:c.*1172G>T	ENSP00000505735.1:n.*1172G>T
ENST00000680832.1:c.*1520G>T	ENSP00000505774.1:n.*1520G>T
ENST00000680929.1:c.*1109G>T	ENSP00000504916.1:n.*1109G>T
ENST00000681108.1:c.*1245+160G>T	ENSP00000506701.1:n.*1245+160G>T
ENST00000681121.1:c.*530G>T	ENSP00000506466.1:n.*530G>T
ENST00000681132.1:c.*1186G>T	ENSP00000506195.1:n.*1186G>T
ENST00000681181.1:c.*1405G>T	ENSP00000506038.1:n.*1405G>T
ENST00000681218.1:c.*1693G>T	ENSP00000505976.1:n.*1693G>T
ENST00000681246.1:c.*1076G>T	ENSP00000505534.1:n.*1076G>T
ENST00000681496.1:c.*1693G>T	ENSP00000505948.1:n.*1693G>T
ENST00000681834.1:n.1759G>T
ENST00000681862.1:c.*1546G>T	ENSP00000505537.1:n.*1546G>T
ENST00000256578.7:c.1582G>T	ENSP00000256578.3:p.Asp528Tyr
ENST00000342115.8:c.1339G>T	ENSP00000345498.4:p.Asp447Tyr
ENST00000358729.8:c.1357G>T	ENSP00000351573.4:p.Asp453Tyr
ENST00000369840.6:c.1493G>T
ENST00000393688.7:c.1225G>T	ENSP00000377292.3:p.Asp409Tyr
ENST00000526301.5:n.1621G>T
ENST00000528454.5:c.1228G>T	ENSP00000437164.1:p.Asp410Tyr
ENST00000528667.5:c.1582G>T	ENSP00000436541.1:p.Asp528Tyr
ENST00000532851.1:n.130G>T
ENST00000533132.1:n.122G>T
NM_001257360.1:c.1582G>T	NP_001244289.1:p.Asp528Tyr
NM_001257361.1:c.1228G>T	NP_001244290.1:p.Asp410Tyr
NM_001308170.1:c.1357G>T	NP_001295099.1:p.Asp453Tyr
NM_004037.7:c.1582G>T	NP_004028.3:p.Asp528Tyr
NM_139156.3:c.1339G>T	NP_631895.1:p.Asp447Tyr
NM_203404.1:c.1225G>T	NP_981949.1:p.Asp409Tyr
XM_011541247.1:c.1795G>T	XP_011539549.1:p.Asp599Tyr
XM_011541248.1:c.1782+160G>T	XP_011539550.1:n.1782+160G>T
XR_946607.1:n.1818G>T
XM_024446431.1:c.1357G>T	XP_024302199.1:p.Asp453Tyr
XM_024446432.1:c.1430+160G>T	XP_024302200.1:n.1430+160G>T
XR_002956282.1:n.1993G>T
NM_001257360.2:c.1582G>T	NP_001244289.1:p.Asp528Tyr
NM_001368809.2:c.1420G>T MANE Select	NP_001355738.1:p.Asp474Tyr
NM_004037.9:c.1420G>T	NP_004028.4:p.Asp474Tyr
NM_001257361.2:c.1228G>T	NP_001244290.1:p.Asp410Tyr
NM_139156.4:c.1339G>T	NP_631895.1:p.Asp447Tyr