Canonical Allele Identifier: CA357241471

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280856C>T (hg19) ; chr4:g.73415139C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415139C>T , CM000666.2:g.73415139C>T	GRCh38
NC_000004.11:g.74280856C>T , CM000666.1:g.74280856C>T	GRCh37
NC_000004.10:g.74499720C>T	NCBI36
NG_009291.1:g.15885C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1163C>T MANE Select	ENSP00000295897.4:p.Ala388Val
ENST00000295897.8:c.1163C>T	ENSP00000295897.4:p.Ala388Val
ENST00000401494.7:c.818C>T	ENSP00000384695.3:p.Ala273Val
ENST00000415165.6:c.587C>T	ENSP00000401820.2:p.Ala196Val
ENST00000476441.6:c.*442C>T	ENSP00000423727.1:n.*442C>T
ENST00000484992.1:n.483C>T
ENST00000503124.5:c.713C>T	ENSP00000421027.1:p.Ala238Val
ENST00000504043.1:n.166C>T
ENST00000505649.5:n.849C>T
ENST00000509063.5:c.1163C>T	ENSP00000422784.1:p.Ala388Val
ENST00000511370.1:c.696C>T
ENST00000621085.4:c.524C>T	ENSP00000483421.1:p.Ala175Val
ENST00000621628.4:c.524C>T	ENSP00000480485.1:p.Ala175Val
NM_000477.5:c.1163C>T	NP_000468.1:p.Ala388Val
NM_000477.6:c.1163C>T	NP_000468.1:p.Ala388Val
NM_000477.7:c.1163C>T MANE Select	NP_000468.1:p.Ala388Val