Canonical Allele Identifier: CA357246140

Gene: ALB

Linked Data

• COSMIC: COSM4940200
• MyVariant Identifiers: chr4:g.74285252C>T (hg19) ; chr4:g.73419535C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419535C>T , CM000666.2:g.73419535C>T	GRCh38
NC_000004.11:g.74285252C>T , CM000666.1:g.74285252C>T	GRCh37
NC_000004.10:g.74504116C>T	NCBI36
NG_009291.1:g.20281C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1681C>T MANE Select	ENSP00000295897.4:p.Pro561Ser
ENST00000295897.8:c.1681C>T	ENSP00000295897.4:p.Pro561Ser
ENST00000401494.7:c.1336C>T	ENSP00000384695.3:p.Pro446Ser
ENST00000415165.6:c.1105C>T	ENSP00000401820.2:p.Pro369Ser
ENST00000476441.6:c.*960C>T	ENSP00000423727.1:n.*960C>T
ENST00000486939.1:n.335C>T
ENST00000503124.5:c.1231C>T	ENSP00000421027.1:p.Pro411Ser
ENST00000505649.5:n.1228C>T
ENST00000508932.5:n.175+80C>T
ENST00000509063.5:c.1681C>T	ENSP00000422784.1:p.Pro561Ser
ENST00000511370.1:c.1214C>T
ENST00000621085.4:c.1042C>T	ENSP00000483421.1:p.Pro348Ser
ENST00000621628.4:c.1042C>T	ENSP00000480485.1:p.Pro348Ser
NM_000477.5:c.1681C>T	NP_000468.1:p.Pro561Ser
NM_000477.6:c.1681C>T	NP_000468.1:p.Pro561Ser
NM_000477.7:c.1681C>T MANE Select	NP_000468.1:p.Pro561Ser