Canonical Allele Identifier: CA1554417250
Gene: CARTPT HGNC NCBI

Linked Data

dbSNP Id: rs1748669079
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71719770G>C , CM000667.2:g.71719770G>C GRCh38
NC_000005.9:g.71015597G>C , CM000667.1:g.71015597G>C GRCh37
NC_000005.8:g.71051353G>C NCBI36
NG_015988.1:g.5608G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000296777.5:c.160-110G>C MANE Select ENSP00000296777.4:n.160-110G>C
ENST00000296777.4:c.160-110G>C ENSP00000296777.4:n.160-110G>C
ENST00000513096.1:n.192G>C
NM_004291.3:c.160-110G>C NP_004282.1:n.160-110G>C
NM_004291.4:c.160-110G>C MANE Select NP_004282.1:n.160-110G>C
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