Canonical Allele Identifier: CA358397283
Gene: GYPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144120555T>G , CM000666.2:g.144120555T>G GRCh38
NC_000004.11:g.145041708T>G , CM000666.1:g.145041708T>G GRCh37
NC_000004.10:g.145261158T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000535709.6:c.65A>C ENSP00000445398.2:p.Glu22Ala
ENST00000641688.3:c.71A>C MANE Select ENSP00000493142.2:p.Glu24Ala
ENST00000642295.1:c.71A>C ENSP00000496079.1:p.Glu24Ala
ENST00000642713.1:c.-8A>C ENSP00000494092.1:n.-8A>C
ENST00000642738.1:c.38-774A>C ENSP00000494322.1:n.38-774A>C
ENST00000643148.1:c.38-3616A>C ENSP00000495505.1:n.38-3616A>C
ENST00000643254.1:n.77-5788A>C
ENST00000646447.1:c.-8A>C ENSP00000495922.1:n.-8A>C
ENST00000324022.14:c.38-774A>C ENSP00000324483.10:n.38-774A>C
ENST00000360771.8:c.71A>C ENSP00000354003.4:p.Glu24Ala
ENST00000503627.2:c.71A>C ENSP00000421243.1:p.Glu24Ala
ENST00000504786.5:c.71A>C ENSP00000425549.1:p.Glu24Ala
ENST00000508337.1:c.*25A>C ENSP00000425719.1:n.*25A>C
ENST00000509346.5:n.129A>C
ENST00000512064.5:c.71A>C ENSP00000426130.1:p.Glu24Ala
ENST00000512789.5:c.38-1803A>C ENSP00000425193.1:n.38-1803A>C
ENST00000514603.1:n.129A>C
ENST00000535709.5:c.65A>C ENSP00000445398.2:p.Glu22Ala
ENST00000616983.4:c.65A>C ENSP00000478329.1:p.Glu22Ala
NM_001308187.1:c.71A>C NP_001295116.1:p.Glu24Ala
NM_001308190.1:c.38-774A>C NP_001295119.1:n.38-774A>C
NM_002099.6:c.71A>C NP_002090.4:p.Glu24Ala
NM_002099.7:c.71A>C NP_002090.4:p.Glu24Ala
XM_017008134.2:c.71A>C XP_016863623.1:p.Glu24Ala
XM_017008135.2:c.-8A>C XP_016863624.1:n.-8A>C
XM_017008136.1:c.38-774A>C XP_016863625.1:n.38-774A>C
XR_002959804.1:n.456+5326T>G
NM_002099.8:c.71A>C MANE Select NP_002090.4:p.Glu24Ala
NM_001308187.2:c.71A>C NP_001295116.1:p.Glu24Ala
NM_001308190.2:c.38-774A>C NP_001295119.1:n.38-774A>C