Canonical Allele Identifier: CA357241236

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280814C>T (hg19) ; chr4:g.73415097C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415097C>T , CM000666.2:g.73415097C>T	GRCh38
NC_000004.11:g.74280814C>T , CM000666.1:g.74280814C>T	GRCh37
NC_000004.10:g.74499678C>T	NCBI36
NG_009291.1:g.15843C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1121C>T MANE Select	ENSP00000295897.4:p.Ala374Val
ENST00000295897.8:c.1121C>T	ENSP00000295897.4:p.Ala374Val
ENST00000401494.7:c.776C>T	ENSP00000384695.3:p.Ala259Val
ENST00000415165.6:c.545C>T	ENSP00000401820.2:p.Ala182Val
ENST00000476441.6:c.*400C>T	ENSP00000423727.1:n.*400C>T
ENST00000484992.1:n.441C>T
ENST00000503124.5:c.671C>T	ENSP00000421027.1:p.Ala224Val
ENST00000504043.1:n.124C>T
ENST00000505649.5:n.807C>T
ENST00000509063.5:c.1121C>T	ENSP00000422784.1:p.Ala374Val
ENST00000511370.1:c.654C>T
ENST00000621085.4:c.491-9C>T	ENSP00000483421.1:n.491-9C>T
ENST00000621628.4:c.487-5C>T	ENSP00000480485.1:n.487-5C>T
NM_000477.5:c.1121C>T	NP_000468.1:p.Ala374Val
NM_000477.6:c.1121C>T	NP_000468.1:p.Ala374Val
NM_000477.7:c.1121C>T MANE Select	NP_000468.1:p.Ala374Val