Canonical Allele Identifier: CA440911858

Gene: ANXA5

Linked Data

• MyVariant Identifiers: chr4:g.122607474T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686319T>G , CM000666.2:g.121686319T>G	GRCh38
NC_000004.11:g.122607474T>G , CM000666.1:g.122607474T>G	GRCh37
NC_000004.10:g.122826924T>G	NCBI36
NG_032042.1:g.15674A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.63A>C MANE Select	ENSP00000296511.5:p.Ala21=
ENST00000296511.9:c.63A>C	ENSP00000296511.5:p.Ala21=
ENST00000501272.6:c.10-2842A>C	ENSP00000424106.1:n.10-2842A>C
ENST00000506395.5:c.63A>C	ENSP00000421421.1:p.Ala21=
ENST00000509016.5:n.184A>C
ENST00000511552.5:n.449A>C
ENST00000513428.5:n.228A>C
ENST00000513523.1:n.231A>C
ENST00000513728.1:c.63A>C	ENSP00000427135.1:p.Ala21=
ENST00000515017.5:c.63A>C	ENSP00000424199.1:p.Ala21=
NM_001154.3:c.63A>C	NP_001145.1:p.Ala21=
XM_017008141.2:c.63A>C	XP_016863630.1:p.Ala21=
NM_001154.4:c.63A>C MANE Select	NP_001145.1:p.Ala21=