Canonical Allele Identifier: CA440911887

Gene: ANXA5

Linked Data

• MyVariant Identifiers: chr4:g.122607498A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121686343A>T , CM000666.2:g.121686343A>T	GRCh38
NC_000004.11:g.122607498A>T , CM000666.1:g.122607498A>T	GRCh37
NC_000004.10:g.122826948A>T	NCBI36
NG_032042.1:g.15650T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.39T>A MANE Select	ENSP00000296511.5:p.Pro13=
ENST00000296511.9:c.39T>A	ENSP00000296511.5:p.Pro13=
ENST00000501272.6:c.10-2866T>A	ENSP00000424106.1:n.10-2866T>A
ENST00000506395.5:c.39T>A	ENSP00000421421.1:p.Pro13=
ENST00000509016.5:n.160T>A
ENST00000511552.5:n.425T>A
ENST00000513428.5:n.204T>A
ENST00000513523.1:n.207T>A
ENST00000513728.1:c.39T>A	ENSP00000427135.1:p.Pro13=
ENST00000515017.5:c.39T>A	ENSP00000424199.1:p.Pro13=
NM_001154.3:c.39T>A	NP_001145.1:p.Pro13=
XM_017008141.2:c.39T>A	XP_016863630.1:p.Pro13=
NM_001154.4:c.39T>A MANE Select	NP_001145.1:p.Pro13=