Canonical Allele Identifier: CA347267717

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717250C>A (hg19) ; chr2:g.73490123C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490123C>A , CM000664.2:g.73490123C>A	GRCh38
NC_000002.11:g.73717250C>A , CM000664.1:g.73717250C>A	GRCh37
NC_000002.10:g.73570758C>A	NCBI36
NG_011690.1:g.109371C>A , LRG_741:g.109371C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682565.1:c.7783C>A	ENSP00000507671.1:p.His2595Asn
ENST00000682801.1:c.7783C>A	ENSP00000507862.1:p.His2595Asn
ENST00000682859.1:c.7783C>A	ENSP00000508222.1:p.His2595Asn
ENST00000683791.1:c.1175C>A
ENST00000684460.1:c.5235C>A
ENST00000684548.1:c.7783C>A	ENSP00000507421.1:p.His2595Asn
ENST00000684590.1:c.2230C>A	ENSP00000507376.1:p.His744Asn
ENST00000684656.1:c.5235C>A
ENST00000613296.6:c.8164C>A MANE Select	ENSP00000482968.1:p.His2722Asn
ENST00000651434.1:c.896-29652C>A
ENST00000423048.5:c.2995C>A	ENSP00000399833.1:p.His999Asn
ENST00000484298.5:c.8038C>A	ENSP00000478155.1:p.His2680Asn
ENST00000613296.4:c.8164C>A	ENSP00000482968.1:p.His2722Asn
ENST00000614410.4:c.8164C>A	ENSP00000479094.1:p.His2722Asn
ENST00000620466.4:n.1967C>A
NM_015120.4:c.8167C>A , LRG_741t1:c.8167C>A	NP_055935.4:p.His2723Asn
NM_001378454.1:c.8164C>A MANE Select	NP_001365383.1:p.His2722Asn