Canonical Allele Identifier: CA357237361

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74274488G>C (hg19) ; chr4:g.73408771G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408771G>C , CM000666.2:g.73408771G>C	GRCh38
NC_000004.11:g.74274488G>C , CM000666.1:g.74274488G>C	GRCh37
NC_000004.10:g.74493352G>C	NCBI36
NG_009291.1:g.9517G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.448G>C MANE Select	ENSP00000295897.4:p.Ala150Pro
ENST00000295897.8:c.448G>C	ENSP00000295897.4:p.Ala150Pro
ENST00000401494.7:c.138-584G>C	ENSP00000384695.3:n.138-584G>C
ENST00000415165.6:c.138-3225G>C	ENSP00000401820.2:n.138-3225G>C
ENST00000441319.5:c.454G>C	ENSP00000392541.1:p.Ala152Pro
ENST00000476441.6:c.80-584G>C	ENSP00000423727.1:n.80-584G>C
ENST00000503124.5:c.33-584G>C	ENSP00000421027.1:n.33-584G>C
ENST00000505649.5:n.134G>C
ENST00000509063.5:c.448G>C	ENSP00000422784.1:p.Ala150Pro
ENST00000510166.5:n.484G>C
ENST00000514786.1:n.417G>C
ENST00000515133.5:n.489G>C
ENST00000621085.4:c.448G>C	ENSP00000483421.1:p.Ala150Pro
ENST00000621628.4:c.448G>C	ENSP00000480485.1:p.Ala150Pro
NM_000477.5:c.448G>C	NP_000468.1:p.Ala150Pro
NM_000477.6:c.448G>C	NP_000468.1:p.Ala150Pro
NM_000477.7:c.448G>C MANE Select	NP_000468.1:p.Ala150Pro