Canonical Allele Identifier: CA439948342

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283852A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418135A>T , CM000666.2:g.73418135A>T	GRCh38
NC_000004.11:g.74283852A>T , CM000666.1:g.74283852A>T	GRCh37
NC_000004.10:g.74502716A>T	NCBI36
NG_009291.1:g.18881A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1476A>T MANE Select	ENSP00000295897.4:p.Pro492=
ENST00000295897.8:c.1476A>T	ENSP00000295897.4:p.Pro492=
ENST00000401494.7:c.1131A>T	ENSP00000384695.3:p.Pro377=
ENST00000415165.6:c.900A>T	ENSP00000401820.2:p.Pro300=
ENST00000476441.6:c.*755A>T	ENSP00000423727.1:n.*755A>T
ENST00000486939.1:n.130A>T
ENST00000503124.5:c.1026A>T	ENSP00000421027.1:p.Pro342=
ENST00000505649.5:n.1023A>T
ENST00000509063.5:c.1476A>T	ENSP00000422784.1:p.Pro492=
ENST00000511370.1:c.1009A>T
ENST00000621085.4:c.837A>T	ENSP00000483421.1:p.Pro279=
ENST00000621628.4:c.837A>T	ENSP00000480485.1:p.Pro279=
NM_000477.5:c.1476A>T	NP_000468.1:p.Pro492=
NM_000477.6:c.1476A>T	NP_000468.1:p.Pro492=
NM_000477.7:c.1476A>T MANE Select	NP_000468.1:p.Pro492=