Canonical Allele Identifier: CA357241403

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280846T>C (hg19) ; chr4:g.73415129T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415129T>C , CM000666.2:g.73415129T>C	GRCh38
NC_000004.11:g.74280846T>C , CM000666.1:g.74280846T>C	GRCh37
NC_000004.10:g.74499710T>C	NCBI36
NG_009291.1:g.15875T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1153T>C MANE Select	ENSP00000295897.4:p.Cys385Arg
ENST00000295897.8:c.1153T>C	ENSP00000295897.4:p.Cys385Arg
ENST00000401494.7:c.808T>C	ENSP00000384695.3:p.Cys270Arg
ENST00000415165.6:c.577T>C	ENSP00000401820.2:p.Cys193Arg
ENST00000476441.6:c.*432T>C	ENSP00000423727.1:n.*432T>C
ENST00000484992.1:n.473T>C
ENST00000503124.5:c.703T>C	ENSP00000421027.1:p.Cys235Arg
ENST00000504043.1:n.156T>C
ENST00000505649.5:n.839T>C
ENST00000509063.5:c.1153T>C	ENSP00000422784.1:p.Cys385Arg
ENST00000511370.1:c.686T>C
ENST00000621085.4:c.514T>C	ENSP00000483421.1:p.Cys172Arg
ENST00000621628.4:c.514T>C	ENSP00000480485.1:p.Cys172Arg
NM_000477.5:c.1153T>C	NP_000468.1:p.Cys385Arg
NM_000477.6:c.1153T>C	NP_000468.1:p.Cys385Arg
NM_000477.7:c.1153T>C MANE Select	NP_000468.1:p.Cys385Arg