Canonical Allele Identifier: CA357241130

Gene: ALB

Linked Data

• COSMIC: COSM6299885
• MyVariant Identifiers: chr4:g.74280783G>A (hg19) ; chr4:g.73415066G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415066G>A , CM000666.2:g.73415066G>A	GRCh38
NC_000004.11:g.74280783G>A , CM000666.1:g.74280783G>A	GRCh37
NC_000004.10:g.74499647G>A	NCBI36
NG_009291.1:g.15812G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1090G>A MANE Select	ENSP00000295897.4:p.Asp364Asn
ENST00000295897.8:c.1090G>A	ENSP00000295897.4:p.Asp364Asn
ENST00000401494.7:c.745G>A	ENSP00000384695.3:p.Asp249Asn
ENST00000415165.6:c.514G>A	ENSP00000401820.2:p.Asp172Asn
ENST00000476441.6:c.*369G>A	ENSP00000423727.1:n.*369G>A
ENST00000484992.1:n.410G>A
ENST00000503124.5:c.640G>A	ENSP00000421027.1:p.Asp214Asn
ENST00000504043.1:n.93G>A
ENST00000505649.5:n.776G>A
ENST00000509063.5:c.1090G>A	ENSP00000422784.1:p.Asp364Asn
ENST00000511370.1:c.623G>A
ENST00000621085.4:c.491-40G>A	ENSP00000483421.1:n.491-40G>A
ENST00000621628.4:c.487-36G>A	ENSP00000480485.1:n.487-36G>A
NM_000477.5:c.1090G>A	NP_000468.1:p.Asp364Asn
NM_000477.6:c.1090G>A	NP_000468.1:p.Asp364Asn
NM_000477.7:c.1090G>A MANE Select	NP_000468.1:p.Asp364Asn