Canonical Allele Identifier: CA357247078

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285980C>A (hg19) ; chr4:g.73420263C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420263C>A , CM000666.2:g.73420263C>A	GRCh38
NC_000004.11:g.74285980C>A , CM000666.1:g.74285980C>A	GRCh37
NC_000004.10:g.74504844C>A	NCBI36
NG_009291.1:g.21009C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1795C>A MANE Select	ENSP00000295897.4:p.Leu599Ile
ENST00000295897.8:c.1795C>A	ENSP00000295897.4:p.Leu599Ile
ENST00000401494.7:c.1450C>A	ENSP00000384695.3:p.Leu484Ile
ENST00000415165.6:c.1219C>A	ENSP00000401820.2:p.Leu407Ile
ENST00000476441.6:c.*1074C>A	ENSP00000423727.1:n.*1074C>A
ENST00000495173.1:n.103C>A
ENST00000503124.5:c.1345C>A	ENSP00000421027.1:p.Leu449Ile
ENST00000505649.5:n.1342C>A
ENST00000508932.5:n.185C>A
ENST00000509063.5:c.1785+624C>A	ENSP00000422784.1:n.1785+624C>A
ENST00000511370.1:c.1328C>A
ENST00000621085.4:c.1156C>A	ENSP00000483421.1:p.Leu386Ile
ENST00000621628.4:c.1156C>A	ENSP00000480485.1:p.Leu386Ile
NM_000477.5:c.1795C>A	NP_000468.1:p.Leu599Ile
NM_000477.6:c.1795C>A	NP_000468.1:p.Leu599Ile
NM_000477.7:c.1795C>A MANE Select	NP_000468.1:p.Leu599Ile