Canonical Allele Identifier: CA2762164691

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413371T>C , CM000666.2:g.73413371T>C	GRCh38
NC_000004.11:g.74279088T>C , CM000666.1:g.74279088T>C	GRCh37
NC_000004.10:g.74497952T>C	NCBI36
NG_009291.1:g.14117T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.844-49T>C MANE Select	ENSP00000295897.4:n.844-49T>C
ENST00000295897.8:c.844-49T>C	ENSP00000295897.4:n.844-49T>C
ENST00000401494.7:c.499-49T>C	ENSP00000384695.3:n.499-49T>C
ENST00000415165.6:c.268-49T>C	ENSP00000401820.2:n.268-49T>C
ENST00000476441.6:c.*123-49T>C	ENSP00000423727.1:n.*123-49T>C
ENST00000484992.1:n.115T>C
ENST00000503124.5:c.394-49T>C	ENSP00000421027.1:n.394-49T>C
ENST00000505649.5:n.530-49T>C
ENST00000509063.5:c.844-49T>C	ENSP00000422784.1:n.844-49T>C
ENST00000511370.1:c.377-49T>C
ENST00000621085.4:c.491-1735T>C	ENSP00000483421.1:n.491-1735T>C
ENST00000621628.4:c.487-1731T>C	ENSP00000480485.1:n.487-1731T>C
NM_000477.5:c.844-49T>C	NP_000468.1:n.844-49T>C
NM_000477.6:c.844-49T>C	NP_000468.1:n.844-49T>C
NM_000477.7:c.844-49T>C MANE Select	NP_000468.1:n.844-49T>C