Canonical Allele Identifier: CA357244177

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283831T>A (hg19) ; chr4:g.73418114T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418114T>A , CM000666.2:g.73418114T>A	GRCh38
NC_000004.11:g.74283831T>A , CM000666.1:g.74283831T>A	GRCh37
NC_000004.10:g.74502695T>A	NCBI36
NG_009291.1:g.18860T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1455T>A MANE Select	ENSP00000295897.4:p.Cys485Ter
ENST00000295897.8:c.1455T>A	ENSP00000295897.4:p.Cys485Ter
ENST00000401494.7:c.1110T>A	ENSP00000384695.3:p.Cys370Ter
ENST00000415165.6:c.879T>A	ENSP00000401820.2:p.Cys293Ter
ENST00000476441.6:c.*734T>A	ENSP00000423727.1:n.*734T>A
ENST00000486939.1:n.109T>A
ENST00000503124.5:c.1005T>A	ENSP00000421027.1:p.Cys335Ter
ENST00000505649.5:n.1002T>A
ENST00000509063.5:c.1455T>A	ENSP00000422784.1:p.Cys485Ter
ENST00000511370.1:c.988T>A
ENST00000621085.4:c.816T>A	ENSP00000483421.1:p.Cys272Ter
ENST00000621628.4:c.816T>A	ENSP00000480485.1:p.Cys272Ter
NM_000477.5:c.1455T>A	NP_000468.1:p.Cys485Ter
NM_000477.6:c.1455T>A	NP_000468.1:p.Cys485Ter
NM_000477.7:c.1455T>A MANE Select	NP_000468.1:p.Cys485Ter