Canonical Allele Identifier: CA357241339

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280834C>G (hg19) ; chr4:g.73415117C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415117C>G , CM000666.2:g.73415117C>G	GRCh38
NC_000004.11:g.74280834C>G , CM000666.1:g.74280834C>G	GRCh37
NC_000004.10:g.74499698C>G	NCBI36
NG_009291.1:g.15863C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1141C>G MANE Select	ENSP00000295897.4:p.Leu381Val
ENST00000295897.8:c.1141C>G	ENSP00000295897.4:p.Leu381Val
ENST00000401494.7:c.796C>G	ENSP00000384695.3:p.Leu266Val
ENST00000415165.6:c.565C>G	ENSP00000401820.2:p.Leu189Val
ENST00000476441.6:c.*420C>G	ENSP00000423727.1:n.*420C>G
ENST00000484992.1:n.461C>G
ENST00000503124.5:c.691C>G	ENSP00000421027.1:p.Leu231Val
ENST00000504043.1:n.144C>G
ENST00000505649.5:n.827C>G
ENST00000509063.5:c.1141C>G	ENSP00000422784.1:p.Leu381Val
ENST00000511370.1:c.674C>G
ENST00000621085.4:c.502C>G	ENSP00000483421.1:p.Leu168Val
ENST00000621628.4:c.502C>G	ENSP00000480485.1:p.Leu168Val
NM_000477.5:c.1141C>G	NP_000468.1:p.Leu381Val
NM_000477.6:c.1141C>G	NP_000468.1:p.Leu381Val
NM_000477.7:c.1141C>G MANE Select	NP_000468.1:p.Leu381Val