Canonical Allele Identifier: CA11491039
Gene: PCYT1A HGNC NCBI
SLC51A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196237816C>T , CM000665.2:g.196237816C>T GRCh38
NC_000003.11:g.195964687C>T , CM000665.1:g.195964687C>T GRCh37
NC_000003.10:g.197449084C>T NCBI36
NG_042817.1:g.54937G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000431016.6:c.*872G>A (PCYT1A) MANE Select ENSP00000394617.1:n.*872G>A
ENST00000292823.6:c.*872G>A (PCYT1A) ENSP00000292823.2:n.*872G>A
ENST00000415111.1:c.58-4678C>T (SLC51A) ENSP00000409560.1:n.58-4678C>T
ENST00000419333.5:c.1084+892G>A (PCYT1A) ENSP00000390968.1:n.1084+892G>A
ENST00000441879.5:c.486+9551G>A (PCYT1A) ENSP00000392397.1:n.486+9551G>A
ENST00000496737.1:n.418-2805C>T (SLC51A)
NM_001312673.1:c.*872G>A (PCYT1A) NP_001299602.1:n.*872G>A
NM_005017.3:c.*872G>A (PCYT1A) NP_005008.2:n.*872G>A
NM_001312673.2:c.*872G>A (PCYT1A) MANE Select NP_001299602.1:n.*872G>A
NM_005017.4:c.*872G>A (PCYT1A) NP_005008.2:n.*872G>A