Canonical Allele Identifier: CA917225970

Gene: ALB

Linked Data

• dbSNP Id: rs1577933697

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404413_73404414insG , CM000666.2:g.73404413_73404414insG	GRCh38
NC_000004.11:g.74270130_74270131insG , CM000666.1:g.74270130_74270131insG	GRCh37
NC_000004.10:g.74488994_74488995insG	NCBI36
NG_009291.1:g.5159_5160insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.79+7_79+8insG MANE Select	ENSP00000295897.4:n.79+7_79+8insG
ENST00000295897.8:c.79+7_79+8insG	ENSP00000295897.4:n.79+7_79+8insG
ENST00000401494.7:c.79+7_79+8insG	ENSP00000384695.3:n.79+7_79+8insG
ENST00000415165.6:c.79+7_79+8insG	ENSP00000401820.2:n.79+7_79+8insG
ENST00000441319.5:c.85+7_85+8insG	ENSP00000392541.1:n.85+7_85+8insG
ENST00000476441.6:c.79+7_79+8insG	ENSP00000423727.1:n.79+7_79+8insG
ENST00000503124.5:c.-102+7_-102+8insG	ENSP00000421027.1:n.-102+7_-102+8insG
ENST00000509063.5:c.79+7_79+8insG	ENSP00000422784.1:n.79+7_79+8insG
ENST00000510166.5:n.120+7_120+8insG
ENST00000514786.1:n.48+77_48+78insG
ENST00000515133.5:n.120+7_120+8insG
ENST00000621085.4:c.79+7_79+8insG	ENSP00000483421.1:n.79+7_79+8insG
ENST00000621628.4:c.79+7_79+8insG	ENSP00000480485.1:n.79+7_79+8insG
NM_000477.5:c.79+7_79+8insG	NP_000468.1:n.79+7_79+8insG
NM_000477.6:c.79+7_79+8insG	NP_000468.1:n.79+7_79+8insG
NM_000477.7:c.79+7_79+8insG MANE Select	NP_000468.1:n.79+7_79+8insG