Canonical Allele Identifier: CA357241093

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280769C>T (hg19) ; chr4:g.73415052C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415052C>T , CM000666.2:g.73415052C>T	GRCh38
NC_000004.11:g.74280769C>T , CM000666.1:g.74280769C>T	GRCh37
NC_000004.10:g.74499633C>T	NCBI36
NG_009291.1:g.15798C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1076C>T MANE Select	ENSP00000295897.4:p.Ala359Val
ENST00000295897.8:c.1076C>T	ENSP00000295897.4:p.Ala359Val
ENST00000401494.7:c.731C>T	ENSP00000384695.3:p.Ala244Val
ENST00000415165.6:c.500C>T	ENSP00000401820.2:p.Ala167Val
ENST00000476441.6:c.*355C>T	ENSP00000423727.1:n.*355C>T
ENST00000484992.1:n.396C>T
ENST00000503124.5:c.626C>T	ENSP00000421027.1:p.Ala209Val
ENST00000504043.1:n.79C>T
ENST00000505649.5:n.762C>T
ENST00000509063.5:c.1076C>T	ENSP00000422784.1:p.Ala359Val
ENST00000511370.1:c.609C>T
ENST00000621085.4:c.491-54C>T	ENSP00000483421.1:n.491-54C>T
ENST00000621628.4:c.487-50C>T	ENSP00000480485.1:n.487-50C>T
NM_000477.5:c.1076C>T	NP_000468.1:p.Ala359Val
NM_000477.6:c.1076C>T	NP_000468.1:p.Ala359Val
NM_000477.7:c.1076C>T MANE Select	NP_000468.1:p.Ala359Val