Canonical Allele Identifier: CA357237372

Gene: ALB

Linked Data

• gnomAD v4: 4-73408772-C-T
• MyVariant Identifiers: chr4:g.74274489C>T (hg19) ; chr4:g.73408772C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408772C>T , CM000666.2:g.73408772C>T	GRCh38
NC_000004.11:g.74274489C>T , CM000666.1:g.74274489C>T	GRCh37
NC_000004.10:g.74493353C>T	NCBI36
NG_009291.1:g.9518C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.449C>T MANE Select	ENSP00000295897.4:p.Ala150Val
ENST00000295897.8:c.449C>T	ENSP00000295897.4:p.Ala150Val
ENST00000401494.7:c.138-583C>T	ENSP00000384695.3:n.138-583C>T
ENST00000415165.6:c.138-3224C>T	ENSP00000401820.2:n.138-3224C>T
ENST00000441319.5:c.455C>T	ENSP00000392541.1:p.Ala152Val
ENST00000476441.6:c.80-583C>T	ENSP00000423727.1:n.80-583C>T
ENST00000503124.5:c.33-583C>T	ENSP00000421027.1:n.33-583C>T
ENST00000505649.5:n.135C>T
ENST00000509063.5:c.449C>T	ENSP00000422784.1:p.Ala150Val
ENST00000510166.5:n.485C>T
ENST00000514786.1:n.418C>T
ENST00000515133.5:n.490C>T
ENST00000621085.4:c.449C>T	ENSP00000483421.1:p.Ala150Val
ENST00000621628.4:c.449C>T	ENSP00000480485.1:p.Ala150Val
NM_000477.5:c.449C>T	NP_000468.1:p.Ala150Val
NM_000477.6:c.449C>T	NP_000468.1:p.Ala150Val
NM_000477.7:c.449C>T MANE Select	NP_000468.1:p.Ala150Val