Canonical Allele Identifier: CA357246717

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285348G>T (hg19) ; chr4:g.73419631G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419631G>T , CM000666.2:g.73419631G>T	GRCh38
NC_000004.11:g.74285348G>T , CM000666.1:g.74285348G>T	GRCh37
NC_000004.10:g.74504212G>T	NCBI36
NG_009291.1:g.20377G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1777G>T MANE Select	ENSP00000295897.4:p.Ala593Ser
ENST00000295897.8:c.1777G>T	ENSP00000295897.4:p.Ala593Ser
ENST00000401494.7:c.1432G>T	ENSP00000384695.3:p.Ala478Ser
ENST00000415165.6:c.1201G>T	ENSP00000401820.2:p.Ala401Ser
ENST00000476441.6:c.*1056G>T	ENSP00000423727.1:n.*1056G>T
ENST00000495173.1:n.85G>T
ENST00000503124.5:c.1327G>T	ENSP00000421027.1:p.Ala443Ser
ENST00000505649.5:n.1324G>T
ENST00000508932.5:n.175+176G>T
ENST00000509063.5:c.1777G>T	ENSP00000422784.1:p.Ala593Ser
ENST00000511370.1:c.1310G>T
ENST00000621085.4:c.1138G>T	ENSP00000483421.1:p.Ala380Ser
ENST00000621628.4:c.1138G>T	ENSP00000480485.1:p.Ala380Ser
NM_000477.5:c.1777G>T	NP_000468.1:p.Ala593Ser
NM_000477.6:c.1777G>T	NP_000468.1:p.Ala593Ser
NM_000477.7:c.1777G>T MANE Select	NP_000468.1:p.Ala593Ser