Canonical Allele Identifier: CA357247080

Gene: ALB

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1795C>G MANE Select	ENSP00000295897.4:p.Leu599Val
ENST00000295897.8:c.1795C>G	ENSP00000295897.4:p.Leu599Val
ENST00000401494.7:c.1450C>G	ENSP00000384695.3:p.Leu484Val
ENST00000415165.6:c.1219C>G	ENSP00000401820.2:p.Leu407Val
ENST00000476441.6:c.*1074C>G	ENSP00000423727.1:n.*1074C>G
ENST00000495173.1:n.103C>G
ENST00000503124.5:c.1345C>G	ENSP00000421027.1:p.Leu449Val
ENST00000505649.5:n.1342C>G
ENST00000508932.5:n.185C>G
ENST00000509063.5:c.1785+624C>G	ENSP00000422784.1:n.1785+624C>G
ENST00000511370.1:c.1328C>G
ENST00000621085.4:c.1156C>G	ENSP00000483421.1:p.Leu386Val
ENST00000621628.4:c.1156C>G	ENSP00000480485.1:p.Leu386Val
NM_000477.5:c.1795C>G	NP_000468.1:p.Leu599Val
NM_000477.6:c.1795C>G	NP_000468.1:p.Leu599Val
NM_000477.7:c.1795C>G MANE Select	NP_000468.1:p.Leu599Val