Canonical Allele Identifier: CA357244447

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283881C>A (hg19) ; chr4:g.73418164C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418164C>A , CM000666.2:g.73418164C>A	GRCh38
NC_000004.11:g.74283881C>A , CM000666.1:g.74283881C>A	GRCh37
NC_000004.10:g.74502745C>A	NCBI36
NG_009291.1:g.18910C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1505C>A MANE Select	ENSP00000295897.4:p.Thr502Lys
ENST00000295897.8:c.1505C>A	ENSP00000295897.4:p.Thr502Lys
ENST00000401494.7:c.1160C>A	ENSP00000384695.3:p.Thr387Lys
ENST00000415165.6:c.929C>A	ENSP00000401820.2:p.Thr310Lys
ENST00000476441.6:c.*784C>A	ENSP00000423727.1:n.*784C>A
ENST00000486939.1:n.159C>A
ENST00000503124.5:c.1055C>A	ENSP00000421027.1:p.Thr352Lys
ENST00000505649.5:n.1052C>A
ENST00000509063.5:c.1505C>A	ENSP00000422784.1:p.Thr502Lys
ENST00000511370.1:c.1038C>A
ENST00000621085.4:c.866C>A	ENSP00000483421.1:p.Thr289Lys
ENST00000621628.4:c.866C>A	ENSP00000480485.1:p.Thr289Lys
NM_000477.5:c.1505C>A	NP_000468.1:p.Thr502Lys
NM_000477.6:c.1505C>A	NP_000468.1:p.Thr502Lys
NM_000477.7:c.1505C>A MANE Select	NP_000468.1:p.Thr502Lys