Canonical Allele Identifier: CA648962850

Gene: ALB

Linked Data

• COSMIC: COSN1300826

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408840_73408841del , CM000666.2:g.73408840_73408841del	GRCh38
NC_000004.11:g.74274557_74274558del , CM000666.1:g.74274557_74274558del	GRCh37
NC_000004.10:g.74493421_74493422del	NCBI36
NG_009291.1:g.9586_9587del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+35_482+36del MANE Select	ENSP00000295897.4:n.482+35_482+36del
ENST00000295897.8:c.482+35_482+36del	ENSP00000295897.4:n.482+35_482+36del
ENST00000401494.7:c.138-515_138-514del	ENSP00000384695.3:n.138-515_138-514del
ENST00000415165.6:c.138-3156_138-3155del	ENSP00000401820.2:n.138-3156_138-3155del
ENST00000441319.5:c.488+35_488+36del	ENSP00000392541.1:n.488+35_488+36del
ENST00000476441.6:c.80-515_80-514del	ENSP00000423727.1:n.80-515_80-514del
ENST00000503124.5:c.33-515_33-514del	ENSP00000421027.1:n.33-515_33-514del
ENST00000505649.5:n.168+35_168+36del
ENST00000509063.5:c.482+35_482+36del	ENSP00000422784.1:n.482+35_482+36del
ENST00000514786.1:n.451+35_451+36del
ENST00000515133.5:n.558_559del
ENST00000621085.4:c.482+35_482+36del	ENSP00000483421.1:n.482+35_482+36del
ENST00000621628.4:c.482+35_482+36del	ENSP00000480485.1:n.482+35_482+36del
NM_000477.5:c.482+35_482+36del	NP_000468.1:n.482+35_482+36del
NM_000477.6:c.482+35_482+36del	NP_000468.1:n.482+35_482+36del
NM_000477.7:c.482+35_482+36del MANE Select	NP_000468.1:n.482+35_482+36del