Canonical Allele Identifier: CA341559117

Gene: AMPD2

Linked Data

• MyVariant Identifiers: chr1:g.110171348G>C (hg19) ; chr1:g.109628726G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109628726G>C , CM000663.2:g.109628726G>C	GRCh38
NC_000001.10:g.110171348G>C , CM000663.1:g.110171348G>C	GRCh37
NC_000001.9:g.109972871G>C	NCBI36
NG_034075.1:g.13914G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256578.8:c.1491G>C	ENSP00000256578.4:p.Trp497Cys
ENST00000358729.9:c.1491G>C	ENSP00000351573.5:p.Trp497Cys
ENST00000369840.7:c.1491G>C	ENSP00000358855.3:p.Trp497Cys
ENST00000474459.6:n.2110G>C
ENST00000476688.3:c.1173G>C	ENSP00000437025.2:p.Trp391Cys
ENST00000486282.7:n.2447G>C
ENST00000524975.2:n.1972G>C
ENST00000525415.2:n.2007G>C
ENST00000526301.6:n.1554G>C
ENST00000527846.7:n.1346G>C
ENST00000528667.7:c.1491G>C MANE Select	ENSP00000436541.2:p.Trp497Cys
ENST00000531203.6:c.1299G>C	ENSP00000431975.2:p.Trp433Cys
ENST00000531734.6:c.1410G>C	ENSP00000433739.2:p.Trp470Cys
ENST00000652975.2:c.*1243G>C	ENSP00000499620.2:n.*1243G>C
ENST00000654851.1:n.1333G>C
ENST00000655992.1:c.1299G>C	ENSP00000499740.1:p.Trp433Cys
ENST00000659122.2:c.1407+231G>C	ENSP00000499621.2:n.1407+231G>C
ENST00000663749.1:c.*1238G>C	ENSP00000499739.1:n.*1238G>C
ENST00000667949.2:c.891G>C	ENSP00000499465.2:p.Trp297Cys
ENST00000668421.1:c.*1432G>C	ENSP00000499362.1:n.*1432G>C
ENST00000679379.1:c.*1243G>C	ENSP00000505528.1:n.*1243G>C
ENST00000679593.1:c.1491G>C	ENSP00000505999.1:p.Trp497Cys
ENST00000679880.1:n.2027G>C
ENST00000679892.1:c.*1259G>C	ENSP00000504882.1:n.*1259G>C
ENST00000679981.1:c.*1505G>C	ENSP00000506422.1:n.*1505G>C
ENST00000680132.1:c.*1441G>C	ENSP00000505950.1:n.*1441G>C
ENST00000680148.1:c.*1243G>C	ENSP00000505994.1:n.*1243G>C
ENST00000680170.1:n.2356G>C
ENST00000680192.1:n.2449G>C
ENST00000680519.1:n.1727G>C
ENST00000680531.1:c.*1238G>C	ENSP00000506332.1:n.*1238G>C
ENST00000680820.1:c.*1243G>C	ENSP00000505735.1:n.*1243G>C
ENST00000680832.1:c.*1591G>C	ENSP00000505774.1:n.*1591G>C
ENST00000680929.1:c.*1180G>C	ENSP00000504916.1:n.*1180G>C
ENST00000681108.1:c.*1245+231G>C	ENSP00000506701.1:n.*1245+231G>C
ENST00000681121.1:c.*601G>C	ENSP00000506466.1:n.*601G>C
ENST00000681132.1:c.*1257G>C	ENSP00000506195.1:n.*1257G>C
ENST00000681181.1:c.*1476G>C	ENSP00000506038.1:n.*1476G>C
ENST00000681218.1:c.*1764G>C	ENSP00000505976.1:n.*1764G>C
ENST00000681246.1:c.*1147G>C	ENSP00000505534.1:n.*1147G>C
ENST00000681496.1:c.*1764G>C	ENSP00000505948.1:n.*1764G>C
ENST00000681834.1:n.1830G>C
ENST00000681862.1:c.*1617G>C	ENSP00000505537.1:n.*1617G>C
ENST00000256578.7:c.1653G>C	ENSP00000256578.3:p.Trp551Cys
ENST00000342115.8:c.1410G>C	ENSP00000345498.4:p.Trp470Cys
ENST00000358729.8:c.1428G>C	ENSP00000351573.4:p.Trp476Cys
ENST00000369840.6:c.1564G>C
ENST00000393688.7:c.1296G>C	ENSP00000377292.3:p.Trp432Cys
ENST00000467071.1:n.13G>C
ENST00000526301.5:n.1692G>C
ENST00000528454.5:c.1299G>C	ENSP00000437164.1:p.Trp433Cys
ENST00000528667.5:c.1653G>C	ENSP00000436541.1:p.Trp551Cys
ENST00000532851.1:n.201G>C
ENST00000533132.1:n.193G>C
NM_001257360.1:c.1653G>C	NP_001244289.1:p.Trp551Cys
NM_001257361.1:c.1299G>C	NP_001244290.1:p.Trp433Cys
NM_001308170.1:c.1428G>C	NP_001295099.1:p.Trp476Cys
NM_004037.7:c.1653G>C	NP_004028.3:p.Trp551Cys
NM_139156.3:c.1410G>C	NP_631895.1:p.Trp470Cys
NM_203404.1:c.1296G>C	NP_981949.1:p.Trp432Cys
XM_011541247.1:c.1866G>C	XP_011539549.1:p.Trp622Cys
XM_011541248.1:c.1782+231G>C	XP_011539550.1:n.1782+231G>C
XR_946607.1:n.1889G>C
XM_024446431.1:c.1428G>C	XP_024302199.1:p.Trp476Cys
XM_024446432.1:c.1430+231G>C	XP_024302200.1:n.1430+231G>C
XR_002956282.1:n.2064G>C
NM_001257360.2:c.1653G>C	NP_001244289.1:p.Trp551Cys
NM_001368809.2:c.1491G>C MANE Select	NP_001355738.1:p.Trp497Cys
NM_004037.9:c.1491G>C	NP_004028.4:p.Trp497Cys
NM_001257361.2:c.1299G>C	NP_001244290.1:p.Trp433Cys
NM_139156.4:c.1410G>C	NP_631895.1:p.Trp470Cys