Canonical Allele Identifier: CA648962858

Gene: ALB

Linked Data

• COSMIC: COSN2044080

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408888_73408891del , CM000666.2:g.73408888_73408891del	GRCh38
NC_000004.11:g.74274605_74274608del , CM000666.1:g.74274605_74274608del	GRCh37
NC_000004.10:g.74493469_74493472del	NCBI36
NG_009291.1:g.9634_9637del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+83_482+86del MANE Select	ENSP00000295897.4:n.482+83_482+86del
ENST00000295897.8:c.482+83_482+86del	ENSP00000295897.4:n.482+83_482+86del
ENST00000401494.7:c.138-467_138-464del	ENSP00000384695.3:n.138-467_138-464del
ENST00000415165.6:c.138-3108_138-3105del	ENSP00000401820.2:n.138-3108_138-3105del
ENST00000441319.5:c.488+83_488+86del	ENSP00000392541.1:n.488+83_488+86del
ENST00000476441.6:c.80-467_80-464del	ENSP00000423727.1:n.80-467_80-464del
ENST00000503124.5:c.33-467_33-464del	ENSP00000421027.1:n.33-467_33-464del
ENST00000505649.5:n.168+83_168+86del
ENST00000509063.5:c.482+83_482+86del	ENSP00000422784.1:n.482+83_482+86del
ENST00000514786.1:n.451+83_451+86del
ENST00000515133.5:n.606_609del
ENST00000621085.4:c.482+83_482+86del	ENSP00000483421.1:n.482+83_482+86del
ENST00000621628.4:c.482+83_482+86del	ENSP00000480485.1:n.482+83_482+86del
NM_000477.5:c.482+83_482+86del	NP_000468.1:n.482+83_482+86del
NM_000477.6:c.482+83_482+86del	NP_000468.1:n.482+83_482+86del
NM_000477.7:c.482+83_482+86del MANE Select	NP_000468.1:n.482+83_482+86del