Canonical Allele Identifier: CA341558949

Gene: AMPD2

Linked Data

• MyVariant Identifiers: chr1:g.110171274T>A (hg19) ; chr1:g.109628652T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109628652T>A , CM000663.2:g.109628652T>A	GRCh38
NC_000001.10:g.110171274T>A , CM000663.1:g.110171274T>A	GRCh37
NC_000001.9:g.109972797T>A	NCBI36
NG_034075.1:g.13840T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256578.8:c.1417T>A	ENSP00000256578.4:p.Ser473Thr
ENST00000358729.9:c.1417T>A	ENSP00000351573.5:p.Ser473Thr
ENST00000369840.7:c.1417T>A	ENSP00000358855.3:p.Ser473Thr
ENST00000474459.6:n.2036T>A
ENST00000476688.3:c.1099T>A	ENSP00000437025.2:p.Ser367Thr
ENST00000486282.7:n.2373T>A
ENST00000524975.2:n.1898T>A
ENST00000525415.2:n.1933T>A
ENST00000526301.6:n.1480T>A
ENST00000527846.7:n.1272T>A
ENST00000528667.7:c.1417T>A MANE Select	ENSP00000436541.2:p.Ser473Thr
ENST00000531203.6:c.1225T>A	ENSP00000431975.2:p.Ser409Thr
ENST00000531734.6:c.1336T>A	ENSP00000433739.2:p.Ser446Thr
ENST00000652975.2:c.*1169T>A	ENSP00000499620.2:n.*1169T>A
ENST00000654851.1:n.1259T>A
ENST00000655992.1:c.1225T>A	ENSP00000499740.1:p.Ser409Thr
ENST00000659122.2:c.1407+157T>A	ENSP00000499621.2:n.1407+157T>A
ENST00000663749.1:c.*1164T>A	ENSP00000499739.1:n.*1164T>A
ENST00000667949.2:c.817T>A	ENSP00000499465.2:p.Ser273Thr
ENST00000668421.1:c.*1358T>A	ENSP00000499362.1:n.*1358T>A
ENST00000679379.1:c.*1169T>A	ENSP00000505528.1:n.*1169T>A
ENST00000679593.1:c.1417T>A	ENSP00000505999.1:p.Ser473Thr
ENST00000679880.1:n.1953T>A
ENST00000679892.1:c.*1185T>A	ENSP00000504882.1:n.*1185T>A
ENST00000679981.1:c.*1431T>A	ENSP00000506422.1:n.*1431T>A
ENST00000680132.1:c.*1367T>A	ENSP00000505950.1:n.*1367T>A
ENST00000680148.1:c.*1169T>A	ENSP00000505994.1:n.*1169T>A
ENST00000680170.1:n.2282T>A
ENST00000680192.1:n.2375T>A
ENST00000680519.1:n.1653T>A
ENST00000680531.1:c.*1164T>A	ENSP00000506332.1:n.*1164T>A
ENST00000680820.1:c.*1169T>A	ENSP00000505735.1:n.*1169T>A
ENST00000680832.1:c.*1517T>A	ENSP00000505774.1:n.*1517T>A
ENST00000680929.1:c.*1106T>A	ENSP00000504916.1:n.*1106T>A
ENST00000681108.1:c.*1245+157T>A	ENSP00000506701.1:n.*1245+157T>A
ENST00000681121.1:c.*527T>A	ENSP00000506466.1:n.*527T>A
ENST00000681132.1:c.*1183T>A	ENSP00000506195.1:n.*1183T>A
ENST00000681181.1:c.*1402T>A	ENSP00000506038.1:n.*1402T>A
ENST00000681218.1:c.*1690T>A	ENSP00000505976.1:n.*1690T>A
ENST00000681246.1:c.*1073T>A	ENSP00000505534.1:n.*1073T>A
ENST00000681496.1:c.*1690T>A	ENSP00000505948.1:n.*1690T>A
ENST00000681834.1:n.1756T>A
ENST00000681862.1:c.*1543T>A	ENSP00000505537.1:n.*1543T>A
ENST00000256578.7:c.1579T>A	ENSP00000256578.3:p.Ser527Thr
ENST00000342115.8:c.1336T>A	ENSP00000345498.4:p.Ser446Thr
ENST00000358729.8:c.1354T>A	ENSP00000351573.4:p.Ser452Thr
ENST00000369840.6:c.1490T>A
ENST00000393688.7:c.1222T>A	ENSP00000377292.3:p.Ser408Thr
ENST00000526301.5:n.1618T>A
ENST00000528454.5:c.1225T>A	ENSP00000437164.1:p.Ser409Thr
ENST00000528667.5:c.1579T>A	ENSP00000436541.1:p.Ser527Thr
ENST00000532851.1:n.127T>A
ENST00000533132.1:n.119T>A
NM_001257360.1:c.1579T>A	NP_001244289.1:p.Ser527Thr
NM_001257361.1:c.1225T>A	NP_001244290.1:p.Ser409Thr
NM_001308170.1:c.1354T>A	NP_001295099.1:p.Ser452Thr
NM_004037.7:c.1579T>A	NP_004028.3:p.Ser527Thr
NM_139156.3:c.1336T>A	NP_631895.1:p.Ser446Thr
NM_203404.1:c.1222T>A	NP_981949.1:p.Ser408Thr
XM_011541247.1:c.1792T>A	XP_011539549.1:p.Ser598Thr
XM_011541248.1:c.1782+157T>A	XP_011539550.1:n.1782+157T>A
XR_946607.1:n.1815T>A
XM_024446431.1:c.1354T>A	XP_024302199.1:p.Ser452Thr
XM_024446432.1:c.1430+157T>A	XP_024302200.1:n.1430+157T>A
XR_002956282.1:n.1990T>A
NM_001257360.2:c.1579T>A	NP_001244289.1:p.Ser527Thr
NM_001368809.2:c.1417T>A MANE Select	NP_001355738.1:p.Ser473Thr
NM_004037.9:c.1417T>A	NP_004028.4:p.Ser473Thr
NM_001257361.2:c.1225T>A	NP_001244290.1:p.Ser409Thr
NM_139156.4:c.1336T>A	NP_631895.1:p.Ser446Thr