Canonical Allele Identifier: CA2581321033
Gene: PITPNC1 HGNC NCBI

Linked Data

dbSNP Id: rs2017854

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.67491905G>T , CM000679.2:g.67491905G>T GRCh38
NC_000017.10:g.65488021G>T , CM000679.1:g.65488021G>T GRCh37
NC_000017.9:g.62918483G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000580974.6:c.49-40897G>T ENSP00000463626.1:n.49-40897G>T
ENST00000581322.6:c.49-40897G>T MANE Select ENSP00000464006.1:n.49-40897G>T
ENST00000299954.13:c.49-40897G>T ENSP00000299954.10:n.49-40897G>T
ENST00000580974.5:c.49-40897G>T ENSP00000463626.1:n.49-40897G>T
ENST00000581322.5:c.49-40897G>T ENSP00000464006.1:n.49-40897G>T
ENST00000584471.5:c.-21-40897G>T ENSP00000464584.1:n.-21-40897G>T
ENST00000584554.1:c.-22+32113G>T ENSP00000464364.1:n.-22+32113G>T
NM_012417.3:c.49-40897G>T NP_036549.2:n.49-40897G>T
NM_181671.2:c.49-40897G>T NP_858057.1:n.49-40897G>T
XM_005257216.2:c.-21-40897G>T XP_005257273.1:n.-21-40897G>T
XM_017024442.1:c.18+34082G>T XP_016879931.1:n.18+34082G>T
XM_017024443.1:c.18+34082G>T XP_016879932.1:n.18+34082G>T
XM_017024444.1:c.-21-40897G>T XP_016879933.1:n.-21-40897G>T
NM_012417.4:c.49-40897G>T MANE Select NP_036549.2:n.49-40897G>T
NM_181671.3:c.49-40897G>T NP_858057.1:n.49-40897G>T