Canonical Allele Identifier: CA357238085

Gene: ALB

Linked Data

• COSMIC: COSM226111
• MyVariant Identifiers: chr4:g.74275100C>T (hg19) ; chr4:g.73409383C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409383C>T , CM000666.2:g.73409383C>T	GRCh38
NC_000004.11:g.74275100C>T , CM000666.1:g.74275100C>T	GRCh37
NC_000004.10:g.74493964C>T	NCBI36
NG_009291.1:g.10129C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.511C>T MANE Select	ENSP00000295897.4:p.Pro171Ser
ENST00000295897.8:c.511C>T	ENSP00000295897.4:p.Pro171Ser
ENST00000401494.7:c.166C>T	ENSP00000384695.3:p.Pro56Ser
ENST00000415165.6:c.138-2613C>T	ENSP00000401820.2:n.138-2613C>T
ENST00000441319.5:c.517C>T	ENSP00000392541.1:p.Pro173Ser
ENST00000476441.6:c.108C>T	ENSP00000423727.1:p.Ile36=
ENST00000503124.5:c.61C>T	ENSP00000421027.1:p.Pro21Ser
ENST00000505649.5:n.197C>T
ENST00000509063.5:c.511C>T	ENSP00000422784.1:p.Pro171Ser
ENST00000511370.1:c.44C>T
ENST00000514786.1:n.480C>T
ENST00000621085.4:c.490+21C>T	ENSP00000483421.1:n.490+21C>T
ENST00000621628.4:c.486+307C>T	ENSP00000480485.1:n.486+307C>T
NM_000477.5:c.511C>T	NP_000468.1:p.Pro171Ser
NM_000477.6:c.511C>T	NP_000468.1:p.Pro171Ser
NM_000477.7:c.511C>T MANE Select	NP_000468.1:p.Pro171Ser