Canonical Allele Identifier: CA357241179

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280796T>G (hg19) ; chr4:g.73415079T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415079T>G , CM000666.2:g.73415079T>G	GRCh38
NC_000004.11:g.74280796T>G , CM000666.1:g.74280796T>G	GRCh37
NC_000004.10:g.74499660T>G	NCBI36
NG_009291.1:g.15825T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1103T>G MANE Select	ENSP00000295897.4:p.Val368Gly
ENST00000295897.8:c.1103T>G	ENSP00000295897.4:p.Val368Gly
ENST00000401494.7:c.758T>G	ENSP00000384695.3:p.Val253Gly
ENST00000415165.6:c.527T>G	ENSP00000401820.2:p.Val176Gly
ENST00000476441.6:c.*382T>G	ENSP00000423727.1:n.*382T>G
ENST00000484992.1:n.423T>G
ENST00000503124.5:c.653T>G	ENSP00000421027.1:p.Val218Gly
ENST00000504043.1:n.106T>G
ENST00000505649.5:n.789T>G
ENST00000509063.5:c.1103T>G	ENSP00000422784.1:p.Val368Gly
ENST00000511370.1:c.636T>G
ENST00000621085.4:c.491-27T>G	ENSP00000483421.1:n.491-27T>G
ENST00000621628.4:c.487-23T>G	ENSP00000480485.1:n.487-23T>G
NM_000477.5:c.1103T>G	NP_000468.1:p.Val368Gly
NM_000477.6:c.1103T>G	NP_000468.1:p.Val368Gly
NM_000477.7:c.1103T>G MANE Select	NP_000468.1:p.Val368Gly