Canonical Allele Identifier: CA439800301

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74280807A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415090A>C , CM000666.2:g.73415090A>C	GRCh38
NC_000004.11:g.74280807A>C , CM000666.1:g.74280807A>C	GRCh37
NC_000004.10:g.74499671A>C	NCBI36
NG_009291.1:g.15836A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1114A>C MANE Select	ENSP00000295897.4:p.Arg372=
ENST00000295897.8:c.1114A>C	ENSP00000295897.4:p.Arg372=
ENST00000401494.7:c.769A>C	ENSP00000384695.3:p.Arg257=
ENST00000415165.6:c.538A>C	ENSP00000401820.2:p.Arg180=
ENST00000476441.6:c.*393A>C	ENSP00000423727.1:n.*393A>C
ENST00000484992.1:n.434A>C
ENST00000503124.5:c.664A>C	ENSP00000421027.1:p.Arg222=
ENST00000504043.1:n.117A>C
ENST00000505649.5:n.800A>C
ENST00000509063.5:c.1114A>C	ENSP00000422784.1:p.Arg372=
ENST00000511370.1:c.647A>C
ENST00000621085.4:c.491-16A>C	ENSP00000483421.1:n.491-16A>C
ENST00000621628.4:c.487-12A>C	ENSP00000480485.1:n.487-12A>C
NM_000477.5:c.1114A>C	NP_000468.1:p.Arg372=
NM_000477.6:c.1114A>C	NP_000468.1:p.Arg372=
NM_000477.7:c.1114A>C MANE Select	NP_000468.1:p.Arg372=