Canonical Allele Identifier: CA357240515

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279170G>T (hg19) ; chr4:g.73413453G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413453G>T , CM000666.2:g.73413453G>T	GRCh38
NC_000004.11:g.74279170G>T , CM000666.1:g.74279170G>T	GRCh37
NC_000004.10:g.74498034G>T	NCBI36
NG_009291.1:g.14199G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.877G>T MANE Select	ENSP00000295897.4:p.Asp293Tyr
ENST00000295897.8:c.877G>T	ENSP00000295897.4:p.Asp293Tyr
ENST00000401494.7:c.532G>T	ENSP00000384695.3:p.Asp178Tyr
ENST00000415165.6:c.301G>T	ENSP00000401820.2:p.Asp101Tyr
ENST00000476441.6:c.*156G>T	ENSP00000423727.1:n.*156G>T
ENST00000484992.1:n.197G>T
ENST00000503124.5:c.427G>T	ENSP00000421027.1:p.Asp143Tyr
ENST00000505649.5:n.563G>T
ENST00000509063.5:c.877G>T	ENSP00000422784.1:p.Asp293Tyr
ENST00000511370.1:c.410G>T
ENST00000621085.4:c.491-1653G>T	ENSP00000483421.1:n.491-1653G>T
ENST00000621628.4:c.487-1649G>T	ENSP00000480485.1:n.487-1649G>T
NM_000477.5:c.877G>T	NP_000468.1:p.Asp293Tyr
NM_000477.6:c.877G>T	NP_000468.1:p.Asp293Tyr
NM_000477.7:c.877G>T MANE Select	NP_000468.1:p.Asp293Tyr