Canonical Allele Identifier: CA2670965540

Gene: ALB

Linked Data

• gnomAD v4: 4-73414956-GTTAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73414959_73414962del , CM000666.2:g.73414959_73414962del	GRCh38
NC_000004.11:g.74280676_74280679del , CM000666.1:g.74280676_74280679del	GRCh37
NC_000004.10:g.74499540_74499543del	NCBI36
NG_009291.1:g.15705_15708del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1059-76_1059-73del MANE Select	ENSP00000295897.4:n.1059-76_1059-73del
ENST00000295897.8:c.1059-76_1059-73del	ENSP00000295897.4:n.1059-76_1059-73del
ENST00000401494.7:c.714-76_714-73del	ENSP00000384695.3:n.714-76_714-73del
ENST00000415165.6:c.483-76_483-73del	ENSP00000401820.2:n.483-76_483-73del
ENST00000476441.6:c.*338-76_*338-73del	ENSP00000423727.1:n.*338-76_*338-73del
ENST00000484992.1:n.379-76_379-73del
ENST00000503124.5:c.609-76_609-73del	ENSP00000421027.1:n.609-76_609-73del
ENST00000504043.1:n.62-76_62-73del
ENST00000505649.5:n.745-76_745-73del
ENST00000509063.5:c.1059-76_1059-73del	ENSP00000422784.1:n.1059-76_1059-73del
ENST00000511370.1:c.592-76_592-73del
ENST00000621085.4:c.491-147_491-144del	ENSP00000483421.1:n.491-147_491-144del
ENST00000621628.4:c.487-143_487-140del	ENSP00000480485.1:n.487-143_487-140del
NM_000477.5:c.1059-76_1059-73del	NP_000468.1:n.1059-76_1059-73del
NM_000477.6:c.1059-76_1059-73del	NP_000468.1:n.1059-76_1059-73del
NM_000477.7:c.1059-76_1059-73del MANE Select	NP_000468.1:n.1059-76_1059-73del