Canonical Allele Identifier: CA439801085

Gene: ALB

Linked Data

• gnomAD v4: 4-73420271-T-A
• MyVariant Identifiers: chr4:g.74285988T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420271T>A , CM000666.2:g.73420271T>A	GRCh38
NC_000004.11:g.74285988T>A , CM000666.1:g.74285988T>A	GRCh37
NC_000004.10:g.74504852T>A	NCBI36
NG_009291.1:g.21017T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1803T>A MANE Select	ENSP00000295897.4:p.Ala601=
ENST00000295897.8:c.1803T>A	ENSP00000295897.4:p.Ala601=
ENST00000401494.7:c.1458T>A	ENSP00000384695.3:p.Ala486=
ENST00000415165.6:c.1227T>A	ENSP00000401820.2:p.Ala409=
ENST00000476441.6:c.*1082T>A	ENSP00000423727.1:n.*1082T>A
ENST00000495173.1:n.111T>A
ENST00000503124.5:c.1353T>A	ENSP00000421027.1:p.Ala451=
ENST00000505649.5:n.1350T>A
ENST00000508932.5:n.193T>A
ENST00000509063.5:c.1785+632T>A	ENSP00000422784.1:n.1785+632T>A
ENST00000511370.1:c.1336T>A
ENST00000621085.4:c.1164T>A	ENSP00000483421.1:p.Ala388=
ENST00000621628.4:c.1164T>A	ENSP00000480485.1:p.Ala388=
NM_000477.5:c.1803T>A	NP_000468.1:p.Ala601=
NM_000477.6:c.1803T>A	NP_000468.1:p.Ala601=
NM_000477.7:c.1803T>A MANE Select	NP_000468.1:p.Ala601=