Canonical Allele Identifier: CA2578111580

Gene: ALB

Linked Data

• gnomAD v4: 4-73408867-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408870_73408871del , CM000666.2:g.73408870_73408871del	GRCh38
NC_000004.11:g.74274587_74274588del , CM000666.1:g.74274587_74274588del	GRCh37
NC_000004.10:g.74493451_74493452del	NCBI36
NG_009291.1:g.9616_9617del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.482+65_482+66del MANE Select	ENSP00000295897.4:n.482+65_482+66del
ENST00000295897.8:c.482+65_482+66del	ENSP00000295897.4:n.482+65_482+66del
ENST00000401494.7:c.138-485_138-484del	ENSP00000384695.3:n.138-485_138-484del
ENST00000415165.6:c.138-3126_138-3125del	ENSP00000401820.2:n.138-3126_138-3125del
ENST00000441319.5:c.488+65_488+66del	ENSP00000392541.1:n.488+65_488+66del
ENST00000476441.6:c.80-485_80-484del	ENSP00000423727.1:n.80-485_80-484del
ENST00000503124.5:c.33-485_33-484del	ENSP00000421027.1:n.33-485_33-484del
ENST00000505649.5:n.168+65_168+66del
ENST00000509063.5:c.482+65_482+66del	ENSP00000422784.1:n.482+65_482+66del
ENST00000514786.1:n.451+65_451+66del
ENST00000515133.5:n.588_589del
ENST00000621085.4:c.482+65_482+66del	ENSP00000483421.1:n.482+65_482+66del
ENST00000621628.4:c.482+65_482+66del	ENSP00000480485.1:n.482+65_482+66del
NM_000477.5:c.482+65_482+66del	NP_000468.1:n.482+65_482+66del
NM_000477.6:c.482+65_482+66del	NP_000468.1:n.482+65_482+66del
NM_000477.7:c.482+65_482+66del MANE Select	NP_000468.1:n.482+65_482+66del