Canonical Allele Identifier: CA358397303

Gene: GYPA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144120567A>T , CM000666.2:g.144120567A>T	GRCh38
NC_000004.11:g.145041720A>T , CM000666.1:g.145041720A>T	GRCh37
NC_000004.10:g.145261170A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000535709.6:c.53T>A	ENSP00000445398.2:p.Leu18Ter
ENST00000641688.3:c.59T>A MANE Select	ENSP00000493142.2:p.Leu20Ter
ENST00000642295.1:c.59T>A	ENSP00000496079.1:p.Leu20Ter
ENST00000642713.1:c.-20T>A	ENSP00000494092.1:n.-20T>A
ENST00000642738.1:c.38-786T>A	ENSP00000494322.1:n.38-786T>A
ENST00000643148.1:c.38-3628T>A	ENSP00000495505.1:n.38-3628T>A
ENST00000643254.1:n.77-5800T>A
ENST00000646447.1:c.-20T>A	ENSP00000495922.1:n.-20T>A
ENST00000324022.14:c.38-786T>A	ENSP00000324483.10:n.38-786T>A
ENST00000360771.8:c.59T>A	ENSP00000354003.4:p.Leu20Ter
ENST00000503627.2:c.59T>A	ENSP00000421243.1:p.Leu20Ter
ENST00000504786.5:c.59T>A	ENSP00000425549.1:p.Leu20Ter
ENST00000508337.1:c.*13T>A	ENSP00000425719.1:n.*13T>A
ENST00000509346.5:n.117T>A
ENST00000512064.5:c.59T>A	ENSP00000426130.1:p.Leu20Ter
ENST00000512789.5:c.38-1815T>A	ENSP00000425193.1:n.38-1815T>A
ENST00000514603.1:n.117T>A
ENST00000535709.5:c.53T>A	ENSP00000445398.2:p.Leu18Ter
ENST00000616983.4:c.53T>A	ENSP00000478329.1:p.Leu18Ter
NM_001308187.1:c.59T>A	NP_001295116.1:p.Leu20Ter
NM_001308190.1:c.38-786T>A	NP_001295119.1:n.38-786T>A
NM_002099.6:c.59T>A	NP_002090.4:p.Leu20Ter
NM_002099.7:c.59T>A	NP_002090.4:p.Leu20Ter
XM_017008134.2:c.59T>A	XP_016863623.1:p.Leu20Ter
XM_017008135.2:c.-20T>A	XP_016863624.1:n.-20T>A
XM_017008136.1:c.38-786T>A	XP_016863625.1:n.38-786T>A
XR_002959804.1:n.456+5338A>T
NM_002099.8:c.59T>A MANE Select	NP_002090.4:p.Leu20Ter
NM_001308187.2:c.59T>A	NP_001295116.1:p.Leu20Ter
NM_001308190.2:c.38-786T>A	NP_001295119.1:n.38-786T>A