Canonical Allele Identifier: CA2789828673
Gene: OAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.124408977_124408978insCTT , CM000672.2:g.124408977_124408978insCTT GRCh38
NC_000010.10:g.126097546_126097547insCTT , CM000672.1:g.126097546_126097547insCTT GRCh37
NC_000010.9:g.126087536_126087537insCTT NCBI36
NG_008861.1:g.14973_14974insAAG , LRG_685:g.14973_14974insAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368845.6:c.200-13_200-12insAAG MANE Select ENSP00000357838.5:n.200-13_200-12insAAG
ENST00000368845.5:c.200-13_200-12insAAG ENSP00000357838.5:n.200-13_200-12insAAG
ENST00000476917.5:n.265-13_265-12insAAG
ENST00000490096.5:n.436-13_436-12insAAG
ENST00000492376.1:n.548-13_548-12insAAG
ENST00000539214.5:c.-215-13_-215-12insAAG ENSP00000439042.1:n.-215-13_-215-12insAAG
NM_000274.3:c.200-13_200-12insAAG , LRG_685t1:c.200-13_200-12insAAG NP_000265.1:n.200-13_200-12insAAG
NM_001171814.1:c.-215-13_-215-12insAAG NP_001165285.1:n.-215-13_-215-12insAAG
XM_006717871.2:c.200-13_200-12insAAG XP_006717934.1:n.200-13_200-12insAAG
XM_011539833.1:c.200-13_200-12insAAG XP_011538135.1:n.200-13_200-12insAAG
XM_011539834.1:c.200-13_200-12insAAG XP_011538136.1:n.200-13_200-12insAAG
NM_001322965.1:c.200-13_200-12insAAG NP_001309894.1:n.200-13_200-12insAAG
NM_001322966.1:c.200-13_200-12insAAG NP_001309895.1:n.200-13_200-12insAAG
NM_001322967.1:c.200-13_200-12insAAG NP_001309896.1:n.200-13_200-12insAAG
NM_001322968.1:c.200-13_200-12insAAG NP_001309897.1:n.200-13_200-12insAAG
NM_001322969.1:c.200-13_200-12insAAG NP_001309898.1:n.200-13_200-12insAAG
NM_001322970.1:c.200-13_200-12insAAG NP_001309899.1:n.200-13_200-12insAAG
NM_001322971.1:c.199+2995_199+2996insAAG NP_001309900.1:n.199+2995_199+2996insAAG
NM_001322974.1:c.-515-13_-515-12insAAG NP_001309903.1:n.-515-13_-515-12insAAG
XM_017016279.1:c.-2254-13_-2254-12insAAG XP_016871768.1:n.-2254-13_-2254-12insAAG
NM_000274.4:c.200-13_200-12insAAG MANE Select NP_000265.1:n.200-13_200-12insAAG
NM_001322965.2:c.200-13_200-12insAAG NP_001309894.1:n.200-13_200-12insAAG
NM_001322966.2:c.200-13_200-12insAAG NP_001309895.1:n.200-13_200-12insAAG
NM_001322967.2:c.200-13_200-12insAAG NP_001309896.1:n.200-13_200-12insAAG
NM_001322968.2:c.200-13_200-12insAAG NP_001309897.1:n.200-13_200-12insAAG
NM_001322969.2:c.200-13_200-12insAAG NP_001309898.1:n.200-13_200-12insAAG
NM_001322970.2:c.200-13_200-12insAAG NP_001309899.1:n.200-13_200-12insAAG
NM_001322971.2:c.199+2995_199+2996insAAG NP_001309900.1:n.199+2995_199+2996insAAG
NM_001322974.2:c.-515-13_-515-12insAAG NP_001309903.1:n.-515-13_-515-12insAAG
NM_001171814.2:c.-215-13_-215-12insAAG NP_001165285.1:n.-215-13_-215-12insAAG