Canonical Allele Identifier: CA439800379

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280872C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415155C>T , CM000666.2:g.73415155C>T	GRCh38
NC_000004.11:g.74280872C>T , CM000666.1:g.74280872C>T	GRCh37
NC_000004.10:g.74499736C>T	NCBI36
NG_009291.1:g.15901C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1179C>T MANE Select	ENSP00000295897.4:p.Cys393=
ENST00000295897.8:c.1179C>T	ENSP00000295897.4:p.Cys393=
ENST00000401494.7:c.834C>T	ENSP00000384695.3:p.Cys278=
ENST00000415165.6:c.603C>T	ENSP00000401820.2:p.Cys201=
ENST00000476441.6:c.*458C>T	ENSP00000423727.1:n.*458C>T
ENST00000484992.1:n.499C>T
ENST00000503124.5:c.729C>T	ENSP00000421027.1:p.Cys243=
ENST00000504043.1:n.182C>T
ENST00000505649.5:n.865C>T
ENST00000509063.5:c.1179C>T	ENSP00000422784.1:p.Cys393=
ENST00000511370.1:c.712C>T
ENST00000621085.4:c.540C>T	ENSP00000483421.1:p.Cys180=
ENST00000621628.4:c.540C>T	ENSP00000480485.1:p.Cys180=
NM_000477.5:c.1179C>T	NP_000468.1:p.Cys393=
NM_000477.6:c.1179C>T	NP_000468.1:p.Cys393=
NM_000477.7:c.1179C>T MANE Select	NP_000468.1:p.Cys393=