Canonical Allele Identifier: CA357247144

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285989G>A (hg19) ; chr4:g.73420272G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420272G>A , CM000666.2:g.73420272G>A	GRCh38
NC_000004.11:g.74285989G>A , CM000666.1:g.74285989G>A	GRCh37
NC_000004.10:g.74504853G>A	NCBI36
NG_009291.1:g.21018G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1804G>A MANE Select	ENSP00000295897.4:p.Ala602Thr
ENST00000295897.8:c.1804G>A	ENSP00000295897.4:p.Ala602Thr
ENST00000401494.7:c.1459G>A	ENSP00000384695.3:p.Ala487Thr
ENST00000415165.6:c.1228G>A	ENSP00000401820.2:p.Ala410Thr
ENST00000476441.6:c.*1083G>A	ENSP00000423727.1:n.*1083G>A
ENST00000495173.1:n.112G>A
ENST00000503124.5:c.1354G>A	ENSP00000421027.1:p.Ala452Thr
ENST00000505649.5:n.1351G>A
ENST00000508932.5:n.194G>A
ENST00000509063.5:c.1785+633G>A	ENSP00000422784.1:n.1785+633G>A
ENST00000511370.1:c.1337G>A
ENST00000621085.4:c.1165G>A	ENSP00000483421.1:p.Ala389Thr
ENST00000621628.4:c.1165G>A	ENSP00000480485.1:p.Ala389Thr
NM_000477.5:c.1804G>A	NP_000468.1:p.Ala602Thr
NM_000477.6:c.1804G>A	NP_000468.1:p.Ala602Thr
NM_000477.7:c.1804G>A MANE Select	NP_000468.1:p.Ala602Thr