Canonical Allele Identifier: CA357244167

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74283828A>C (hg19) ; chr4:g.73418111A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418111A>C , CM000666.2:g.73418111A>C	GRCh38
NC_000004.11:g.74283828A>C , CM000666.1:g.74283828A>C	GRCh37
NC_000004.10:g.74502692A>C	NCBI36
NG_009291.1:g.18857A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1452A>C MANE Select	ENSP00000295897.4:p.Leu484Phe
ENST00000295897.8:c.1452A>C	ENSP00000295897.4:p.Leu484Phe
ENST00000401494.7:c.1107A>C	ENSP00000384695.3:p.Leu369Phe
ENST00000415165.6:c.876A>C	ENSP00000401820.2:p.Leu292Phe
ENST00000476441.6:c.*731A>C	ENSP00000423727.1:n.*731A>C
ENST00000486939.1:n.106A>C
ENST00000503124.5:c.1002A>C	ENSP00000421027.1:p.Leu334Phe
ENST00000505649.5:n.999A>C
ENST00000509063.5:c.1452A>C	ENSP00000422784.1:p.Leu484Phe
ENST00000511370.1:c.985A>C
ENST00000621085.4:c.813A>C	ENSP00000483421.1:p.Leu271Phe
ENST00000621628.4:c.813A>C	ENSP00000480485.1:p.Leu271Phe
NM_000477.5:c.1452A>C	NP_000468.1:p.Leu484Phe
NM_000477.6:c.1452A>C	NP_000468.1:p.Leu484Phe
NM_000477.7:c.1452A>C MANE Select	NP_000468.1:p.Leu484Phe