Canonical Allele Identifier: CA2670936927

Gene: ALB

Linked Data

• gnomAD v4: 4-73408462-TGGGAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408467_73408471del , CM000666.2:g.73408467_73408471del	GRCh38
NC_000004.11:g.74274184_74274188del , CM000666.1:g.74274184_74274188del	GRCh37
NC_000004.10:g.74493048_74493052del	NCBI36
NG_009291.1:g.9213_9217del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.271-127_271-123del MANE Select	ENSP00000295897.4:n.271-127_271-123del
ENST00000295897.8:c.271-127_271-123del	ENSP00000295897.4:n.271-127_271-123del
ENST00000401494.7:c.138-888_138-884del	ENSP00000384695.3:n.138-888_138-884del
ENST00000415165.6:c.137+3294_137+3298del	ENSP00000401820.2:n.137+3294_137+3298del
ENST00000441319.5:c.277-127_277-123del	ENSP00000392541.1:n.277-127_277-123del
ENST00000476441.6:c.80-888_80-884del	ENSP00000423727.1:n.80-888_80-884del
ENST00000503124.5:c.33-888_33-884del	ENSP00000421027.1:n.33-888_33-884del
ENST00000509063.5:c.271-127_271-123del	ENSP00000422784.1:n.271-127_271-123del
ENST00000510166.5:n.307-127_307-123del
ENST00000514786.1:n.240-127_240-123del
ENST00000515133.5:n.312-127_312-123del
ENST00000621085.4:c.271-127_271-123del	ENSP00000483421.1:n.271-127_271-123del
ENST00000621628.4:c.271-127_271-123del	ENSP00000480485.1:n.271-127_271-123del
NM_000477.5:c.271-127_271-123del	NP_000468.1:n.271-127_271-123del
NM_000477.6:c.271-127_271-123del	NP_000468.1:n.271-127_271-123del
NM_000477.7:c.271-127_271-123del MANE Select	NP_000468.1:n.271-127_271-123del