Canonical Allele Identifier: CA648962472

Gene: ALB

Linked Data

• COSMIC: COSN2044065

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404429_73404431del , CM000666.2:g.73404429_73404431del	GRCh38
NC_000004.11:g.74270146_74270148del , CM000666.1:g.74270146_74270148del	GRCh37
NC_000004.10:g.74489010_74489012del	NCBI36
NG_009291.1:g.5175_5177del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.79+23_79+25del MANE Select	ENSP00000295897.4:n.79+23_79+25del
ENST00000295897.8:c.79+23_79+25del	ENSP00000295897.4:n.79+23_79+25del
ENST00000401494.7:c.79+23_79+25del	ENSP00000384695.3:n.79+23_79+25del
ENST00000415165.6:c.79+23_79+25del	ENSP00000401820.2:n.79+23_79+25del
ENST00000441319.5:c.85+23_85+25del	ENSP00000392541.1:n.85+23_85+25del
ENST00000476441.6:c.79+23_79+25del	ENSP00000423727.1:n.79+23_79+25del
ENST00000503124.5:c.-102+23_-102+25del	ENSP00000421027.1:n.-102+23_-102+25del
ENST00000509063.5:c.79+23_79+25del	ENSP00000422784.1:n.79+23_79+25del
ENST00000510166.5:n.120+23_120+25del
ENST00000514786.1:n.48+93_48+95del
ENST00000515133.5:n.120+23_120+25del
ENST00000621085.4:c.79+23_79+25del	ENSP00000483421.1:n.79+23_79+25del
ENST00000621628.4:c.79+23_79+25del	ENSP00000480485.1:n.79+23_79+25del
NM_000477.5:c.79+23_79+25del	NP_000468.1:n.79+23_79+25del
NM_000477.6:c.79+23_79+25del	NP_000468.1:n.79+23_79+25del
NM_000477.7:c.79+23_79+25del MANE Select	NP_000468.1:n.79+23_79+25del