Canonical Allele Identifier: CA2651001365

Gene: GNPAT

Linked Data

• gnomAD v4: 1-231277755-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231277755T>C , CM000663.2:g.231277755T>C	GRCh38
NC_000001.10:g.231413501T>C , CM000663.1:g.231413501T>C	GRCh37
NC_000001.9:g.229480124T>C	NCBI36
NG_008240.1:g.41583T>C
NG_008240.2:g.41583T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366647.9:c.*213T>C MANE Select	ENSP00000355607.4:n.*213T>C
ENST00000644483.1:c.*1942T>C	ENSP00000496537.1:n.*1942T>C
ENST00000366647.8:c.*213T>C	ENSP00000355607.4:n.*213T>C
NM_001316350.1:c.*213T>C	NP_001303279.1:n.*213T>C
NM_014236.3:c.*213T>C	NP_055051.1:n.*213T>C
XM_005273313.3:c.*213T>C	XP_005273370.1:n.*213T>C
XM_011544303.1:c.*213T>C	XP_011542605.1:n.*213T>C
XM_011544304.1:c.*213T>C	XP_011542606.1:n.*213T>C
XM_005273313.4:c.*213T>C	XP_005273370.1:n.*213T>C
XM_011544303.3:c.*213T>C	XP_011542605.1:n.*213T>C
XM_011544304.2:c.*213T>C	XP_011542606.1:n.*213T>C
NM_014236.4:c.*213T>C MANE Select	NP_055051.1:n.*213T>C
NM_001316350.2:c.*213T>C	NP_001303279.1:n.*213T>C