Canonical Allele Identifier: CA357246700

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74285345T>C (hg19) ; chr4:g.73419628T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419628T>C , CM000666.2:g.73419628T>C	GRCh38
NC_000004.11:g.74285345T>C , CM000666.1:g.74285345T>C	GRCh37
NC_000004.10:g.74504209T>C	NCBI36
NG_009291.1:g.20374T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1774T>C MANE Select	ENSP00000295897.4:p.Phe592Leu
ENST00000295897.8:c.1774T>C	ENSP00000295897.4:p.Phe592Leu
ENST00000401494.7:c.1429T>C	ENSP00000384695.3:p.Phe477Leu
ENST00000415165.6:c.1198T>C	ENSP00000401820.2:p.Phe400Leu
ENST00000476441.6:c.*1053T>C	ENSP00000423727.1:n.*1053T>C
ENST00000495173.1:n.82T>C
ENST00000503124.5:c.1324T>C	ENSP00000421027.1:p.Phe442Leu
ENST00000505649.5:n.1321T>C
ENST00000508932.5:n.175+173T>C
ENST00000509063.5:c.1774T>C	ENSP00000422784.1:p.Phe592Leu
ENST00000511370.1:c.1307T>C
ENST00000621085.4:c.1135T>C	ENSP00000483421.1:p.Phe379Leu
ENST00000621628.4:c.1135T>C	ENSP00000480485.1:p.Phe379Leu
NM_000477.5:c.1774T>C	NP_000468.1:p.Phe592Leu
NM_000477.6:c.1774T>C	NP_000468.1:p.Phe592Leu
NM_000477.7:c.1774T>C MANE Select	NP_000468.1:p.Phe592Leu