Canonical Allele Identifier: CA357238091

Gene: ALB

Linked Data

• gnomAD v4: 4-73409387-A-C
• MyVariant Identifiers: chr4:g.74275104A>C (hg19) ; chr4:g.73409387A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409387A>C , CM000666.2:g.73409387A>C	GRCh38
NC_000004.11:g.74275104A>C , CM000666.1:g.74275104A>C	GRCh37
NC_000004.10:g.74493968A>C	NCBI36
NG_009291.1:g.10133A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.515A>C MANE Select	ENSP00000295897.4:p.Tyr172Ser
ENST00000295897.8:c.515A>C	ENSP00000295897.4:p.Tyr172Ser
ENST00000401494.7:c.170A>C	ENSP00000384695.3:p.Tyr57Ser
ENST00000415165.6:c.138-2609A>C	ENSP00000401820.2:n.138-2609A>C
ENST00000441319.5:c.521A>C	ENSP00000392541.1:p.Tyr174Ser
ENST00000476441.6:c.112A>C	ENSP00000423727.1:p.Thr38Pro
ENST00000503124.5:c.65A>C	ENSP00000421027.1:p.Tyr22Ser
ENST00000505649.5:n.201A>C
ENST00000509063.5:c.515A>C	ENSP00000422784.1:p.Tyr172Ser
ENST00000511370.1:c.48A>C
ENST00000514786.1:n.484A>C
ENST00000621085.4:c.490+25A>C	ENSP00000483421.1:n.490+25A>C
ENST00000621628.4:c.486+311A>C	ENSP00000480485.1:n.486+311A>C
NM_000477.5:c.515A>C	NP_000468.1:p.Tyr172Ser
NM_000477.6:c.515A>C	NP_000468.1:p.Tyr172Ser
NM_000477.7:c.515A>C MANE Select	NP_000468.1:p.Tyr172Ser